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acetylcholine receptor antibody

acute intermittant porphyria

adrenergic blocker

adult polyglucosan body disease

adverse drug reaction

alpha adrenergic blocker

Alzheimer's disease

amphiphysin antibodies

amyotrophic lateral sclerosis

antibodies to voltage-gated calcium channels

antiganglioside antibodies

antineurofascin antibodies

ataxia, cerebellar

ataxia, progressive

autoimmune autonomic ganglionopathy

autoimmune disease

autonomic cardiovascular reflexes

autonomic dysfunction

autonomic dysfunction, acute

autonomic dysfunction, evaluation of

autonomic nervous system

autonomic neuropathy

autosomal dominant leukodystrophy

axonal degeneration

bladder dysfunction

botulinum toxin

botulism antitoxin

botulism immune globulin

botulism, infant

bulbar palsy, acute

burning paresthesia

campylobacter infection

carcinoma of lung

CAT scan, abnormal

CAT scan, chest

CAT scan, emission, abnormal

cerebellar degeneration

cerebellar lesion

cerebellar vermis

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, oligoclonal IgG in

chewing movements

cingulate island sign

Clinical Pathologic Conference(C.P.C.)

coat-hanger pain

cogwheel rigidty

collapsin response mediator protein 5 IgG

contactin associated protein like 1 antibodies

contactin associated protein like 2 antibodies

corpus callosum

corpus callosum, lesion of

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

cyst, arachnoid, infant

deep tendon reflexes

degenerative diseases of CNS

delay in diagnosis

dementia, familial

dementia, rapidly progressive

dementia, subcortical

dermatomyositis

diabetes mellitus

diabetes mellitus, chemical

dialysis dementia

dialysis disequilibrium syndrome

differential diagnosis

distal muscle atrophy

distal muscle weakness

dysdiadochokinesia

electroencephalogram, abnormalities of

electromyogram, incremental response

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, paraneoplastic

encephalomyelitis

epidemiology of neurology

erectile dysfunction

exercise-related muscle strength increase

exome sequencing

extrapyramidal movement disorder, progressive

facial asymmetry

facial weakness

facial weakness, bilateral

fatal familial insomnia

feeding disorder

Fisher's syndrome

flaccid paralysis

fludrocortisone

food-borne infection

gammaglobulin therapy, intravenous

gammaglobulin therapy, intravenous, refractory

genetic neurologic disorders

genetic testing

glucose tolerance test, abnormal

glycogen storage disease

Guillain Barre syndrome

Guillain Barre syndrome, axonal form

Guillain Barre syndrome, complications

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, etiology of

Guillain Barre syndrome, prognosis of

Guillain Barre syndrome, variant forms of

hallucination, auditory

heat intolerance

hemifacial atrophy

heralding manifestation

Horner's syndrome

H-reflex testing

hyperamylasemia

hypokalemic paralysis

hypoosmolality of serum

hypotension, neurologic causes of

hypotension, systemic

hypotonia, infants

IgG4-related disease

ileus, paralytic

imbalance, postural

immunologic disease

immunology and the nervous system

inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

infant, evaluation of

intellectual deficit

intellectual deterioration

intrinsic hand muscles, wasting of

juvenile distal and segmental muscular atrophy

laughing, pathologic

leg weakness, bilateral

leucine rich glioma inactivated 1 antibodies

leukoencephalopathy

life expectancy

light-near dissociation, causes of

limbic encephalitis

livedo reticularis

malignancy screen

malignancy, occult

marche a petits pas

memory, defect of recent

memory, impairment of

mental status, abnormal

metabolic disorder, primary

middle cerebellar peduncle, lesion, bilateral

Mini Mental Status Examination

monoamine oxidase inhibitors

mononeuritis multiplex

Morvan's fibrillary chorea

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI, contrast enhanced

MRI, diffusion weighted

MRI, lumbosacral plexus

multiple sclerosis

multiple system atrophy

muscle atrophy, progressive

muscle strength, testing

muscle twitching

muscle weakness

muscle weakness, proximal

muscle weakness, sudden onset of

myasthenia gravis

myasthenia gravis, paraneoplastic

myasthenic syndrome

myeloneuropathy

myelopathy, necrotizing

myoclonic jerks

nausea and vomiting

nephrotic syndrome

nerve conduction studies

nerve growth factor

nerve growth stimulating activity

nerve root enhancement

nerve root hypertrophy

neurofibromatosis 1

neurogenic bladder

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic signs

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuronal cell surface antigen

neuronal intranuclear inclusion disease

neuronopathy, sensory

neuropathy, amyloid

neuropathy, autoimmune

neuropathy, hereditary peripheral

neuropathy, painful

neuropathy, paraneoplastic

neuropathy, peripheral

neuropathy, sensory

neuropathy, sensory, hereditary

neuroprotective agents

next-generation sequencing

NMDA antagonists

node of Ranvier

nodopathy, autoimmune

ocular dysmetria

onconeural antibodies

ophthalmoplegia

ophthalmoplegia, acute

ophthalmoplegia, bilateral, acute

ophthalmoplegia, total

opsoclonus-myoclonus syndrome

optic neuropathy

oral contraceptives

orthostatic hypotension

orthostatic hypotension, idiopathic

orthostatic hypotension, treatment of

pain, abdominal

palate, paralysis

paralysis, acute areflexic

paraneoplastic cerebellar degeneration

Parkinson disease

Parkinson disease, atypical

Parkinson disease, differential diagnosis of

Parkinson disease, familial

Parkinson disease, L-dopa nonresponsive

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

paroxysmal neurologic deficits

peripheral nerve, lesion of

pheochromocytoma

physical therapy

pleocytosis of cerebrospinal fluid

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polyneuropathy, uremic

posterior leukoencephalopathy syndrome

postural abnormality

prevention of neurologic disorders

progressive hemifacial atrophy

progressive neurologic disorder

progressive supranuclear palsy

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychological testing

psychosis, acute

psychotic behavior

ptosis, bilateral

pulmonary embolism

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pupil, dilated, bilateral

pupil, light reflex, abnormal

pure autonomic failure

pyramidal tract

pyramidal tract dysfunction

reflex sympathetic dystrophy

reflex sympathetic dystrophy, children

remote effect of cancer on the nervous system

renal transplantation

renal tubular acidosis

repetitive nerve stimulation

respiratory failure

Riley-Day syndrome

salivation, excessive

scleroderma, neurologic involvement with

sensory ganglia

serum lipase, elevated

shoulder, pain in

Shy-Drager syndrome

single-fiber electromyography

Sjogren's syndrome

skin, temperature difference

sleep pathology and physiology

SNCA duplication

spinal cord, lesion of

steroid therapy, CNS treatment and complications with

subcortical U fibers

sweating, abnormality of

sympathetic block

sympathetic nervous system

sympathomimetic drugs

synucleinopathy

systemic illness

tandem gait, ataxic

tensilon test, false positive

thalamus, lesion of-bilateral

tongue, impaired movements of

tongue, weakness

treatment of neurologic disorder

trinucleotide repeats

uremic encephalopathy

urinary frequency

urinary incontinence

urinary retention

urine osmolality, elevated

viral infection

vision, blurred

vocal cord paralysis

walking, difficulty with

Watson-Schwartz reaction

weakness, acute

weakness, generalized

weakness, infant

weakness, progressive

weakness, proximal

white matter disease

wide based gait

Showing articles 3400 to 3450 of 3776 << Previous Next >>

Hypersomnia Associated with Alveolar Hypoventilation in Myotonic Dystrophy
Neurol 31:1336-1337, Hansotia,P.,et al, 1981

Progressive Infantile Poliodystrophy, Assoc. With Disturbed Pyruvate Oxidation in Muscle & Liver
Arch Neurol 38:767-772, Prick,M.J.J.,et al, 1981

Biotin For Neurologic Disorders of Uremia
NEJM 304:764, Yatzidis,H.,et al, 1981

Neurologic Complications of Hyperthyroidism
Arch Neurol 38:669-670, Bulens,C., 1981

Amitriptyline-induced Ophthalmoplegia
Neurol 31:1188-1190, Spector,R.H.,et al, 1981

MS & Allied Demyelinative Diseases, in Principles of Neurology
McGraw-Hill Book Co, 1981, p. 647., Adams,R.D.&Victor,M., 1981

Intracardiac Electrophysiologic Techniques in Recurrent Syncope of Unknown Cause
Ann Int Med 95:542-548, DiMarco,J.P.,et al, 1981

CNS Manifestations of the Hemolytic-Uremic Syndrome
Am J Dis Child 134:869-872, Bale,J.F.,et al, 1980

Computerised Tomography as an Indication of Long-Term Outcome After Acute Carbon Monoxide Poisoning
Lancet 1:783-784, Sawada,Y.,et al, 1980

Acute Carbon Monoxide Poisoning:Computed Tomography of the Brain
AJNR 1:399-402, Kim,K.S.,et al, 1980

Neurological Disease In Ex-Far-East Prisoners Of War
Lancet 2:135-137, Gibberd,F.B.,et al, 1980

Kernicterus & Central Pontine Myelinolysis in a 14-year-old Boy with Fulminating Viral Hepatitis
Ann Neurol 8:633-636, Ho,K-C.,et al, 1980

Child Abuse as a Cause of Post-Traumatic Hypopituitarism
NEJM 302:724-728, Miller,W.L.,et al, 1980

Multiple Vertebral Hemangiomas Resembling Metastases with Spinal Cord Compression
Arch Neurol 37:247-248, Zito,G.,et al, 1980

Protein Binding of Valproic Acid in Uremic Patient
Neurol 30:557-559, Bruni,J.,et al, 1980

Acute Ataxia Associated with Ciguatera-type (Grouper) Tropical Fish Poisoning, Letter
Ann Neurol 7:491, Jones,H.R.Jr., 1980

Demyelinating Radiculopathy in the Kearns-Sayre Syndrome:A Clinicopathological Study
Ann Neurol 8:373-380, Groothuis,D.R.,et al, 1980

Infantile Neuronal Degeneration Masquerading as Werdnig-Hoffmann Disease
Ann Neurol 8:317-324, Steiman,G.S.,et al, 1980

Postlaminectomy Arteriovenous Fistula, Suspected From Right-Side Heart Cath
Arch Int Med 140:1168-1169, Thompson,J.A.,et al, 1980

Fetal Hydantoin Syndrome, Neuroblastoma, & Hemorrhagic Disease in a Neonate
Jr. , et al, JAMA 244:1464-146580., Allen,R.W., 1980

Congestive Heart Failure During Carbamazepine Therapy
Ann Neurol 8:200-201, Terrence,C.F.,et al, 1980

EEG in Dialysis Encephalopathy
Neurol 30:1148-1154, Hughes,J.R.,et al, 1980

Proximal Muscle Weakness in Uremia
Arch Neurol 37:555-558, Lazaro,R.P.,et al, 1980

Pseudotumor Cerebri, Clinical Profile & Visual Outcome in 63 Patients
Mayo Clin Proc 55:541-546, Rush,J.A., 1980

Dysconjugate Gaze in Hepatic Coma
Ann Neurol 8:328-329, Caplan,L.R.,et al, 1980

Fatal Myeloencephalopathy Caused by Intrathecal Vincristine
Neurol 30:867-871, Slyter,H.,et al, 1980

Hypokalemic Periodic Paralysis in Chronic Toluene Exposure
Arch Neurol 37:673, Bennett,R.H.,et al, 1980

Clinical Criteria for Diagnosis of Machado-Joseph Disease:Report of a Non-Azorean Portuguese Family
Neurol 30:319-322, Lima,L.,et al, 1980

Progressive Bulbar Paralysis Associated With Neurgl Deafness, A Nosological Entity
Arch Neurol 37:214-216, Alberica,R.,et al, 1980

Ocular Myasthenia:Diagnosis & Therapy
In Neuro-Ophthalmology, Vol X ed. by J. Glaser. CV Mosby Co, St. Louis, Daroff,R., 1980

Clin. Path. Conference
Lymphoplasmacytic Intersitial Pneumonitis, Progressive Multifocal Leukoencephalopathy. Case Record 1, -10,NEJM 302:795,1980., 1980

Electrocardiogram Abnormalities in Carriers of Duchenne Muscular Dystrophy
Neurol 30:497-501, Lane,R.J.M.,et al, 1980

Echocardiographic Evaluation of Cardiac Abnormalities in Duchenne's Dystrophy & Myotonic Muscular Dystrophy
Arch Neurol 37:273-277, Reeves,W.C.,et al, 1980

Neuropathy & Mitochondrial Myopathy
Ann Neurol 7:262-268, Peyronnard,M.J.,et al, 1980

Baclofen in Treatment of the"Stiff-Man Syndrome
Arch Neurol 37:600-601, Whelan,J.L., 1980

Chronic Migrainous Neuralgia, A Variant Of Cluster Headache
Brain 103:149-159, Pearce,J.M.S., 1980

Lithium Carbonate Therapy for Cluster Headache, Changes in Number of Platelets, & Serotonin & Hista
Arch Neurol 37:559-563, Medina,J.L.,et al, 1980

"Sinutabs"For Cluster Headache
NEJM 303:107-108, Cohen,K.L., 1980

Progressive Multifocal Leukoencephalopathy
Arch Neurol 37:497-501, Boudewijn,A.C.,et al, 1980

The Not-So-Benign Miller Fisher Syndrome, A Variant of the Guillain-Barre Syndrome
Arch Neurol 37:384-385, Blau,I.,et al, 1980

Acne Fulminans with Inflammatory Myopathy
Neurol 8:67-69, Noseworthy,J.H.,et al, 1980

Gross Demonstration of Atrophic Cauda Equina Roots in Motor Neuron Disease, An Improved Method
Arch Neurol 37:394, Meneses,A., 1980

Osteopetrosis, Renal Tubular Acidosis & Basal Ganglia Calcification in Three Sisters
Am J Med 69:64-74, Whythe,M.P.,et al, 1980

Dialysis Encephalopathy in Peritoneal Dialysis
JAMA 244:365-366, Smith,D.B.,et al, 1980

Use of Adrenal Biopsy in Diagnosing Adreno-leukomyeloneuropathy
Arch Neurol 37:634-636, Weiss,G.M.,et al, 1980

Mitral Valve Prolapse & Ophthalmoplegia:A Progressive, Cardioneurologic Syndrome
Ann Int Med 92:735-741, Darsee,J.R.,et al, 1980

Headaches
NEJM 302:446-450, Caviness,V.S.,et al, 1980

Myotonic Dystrophy
In Harrison's Principles of Internal Medicine, 9th Ed, McGraw-Hill Book Co, NY 206180., Adams,R.D.,et al, 1980

Leukaemia:Neurological Involvement
in Handbk of Clinical Neurology, Vinkin PJ & Bruyn GW, Ed, North-Holland Publ Co, Amsterdam 39:1, Yuill,G.M., 1980

Neurologic Manifestations in Macroglobulinemia
In Vinken PJ, Bruyn GW, Eds, Handbook of Clin Neurol, Vol 39, North-Holland Publ Co, p. 189, Abramsky,O., 1980

Showing articles 3400 to 3450 of 3776 << Previous Next >>